Salaire moyen: CHF24 144 /annuel
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- ...Manpower Für einen unserer Pharma-Kunden mit Sitz in Visp suchen wir einen Process Engineer . Description: Ihre Aufgaben: ? Planung und Realisierung von Teil- und Kleinprojekten, z. B. verfahrenstechnische Berechnungen und Optimierungen in der Anlage...SuggéréRemplaçant
- ...For our client, an international company based in Stein, we are looking for a Process Automation Engineer to support growth projects and ensure the successful delivery of automated systems. The Process Automation Engineer plays a key role in the delivery of growth projects...SuggéréRecrutement immédiat
- ...Your mission We are looking for an Experienced Qualification Engineer to play a defining role in our ambitious expansion in Visp.... ...engineering pharmaceutical technology medical technology chemistry process engineering or similar or completed technical or scientific...SuggéréTemps plein
- ...Ihre Aufgaben Planung und Durchführung von technischen Teilprojekten im Anlagenumfeld, inkl. Prozessoptimierung und Engineering-Berechnungen Erstellung von Machbarkeitsanalysen und Konzeptstudien für Neu- und Umbauten, inkl. Budget- und Zeitplanung Durchführung...SuggéréTemps plein
- Senior Bioprocess Engineer (Biologics) Location: Visp, Switzerland — 100% on-site Function: Operations / Manufacturing Science & Technology... ...logistics; support delivery of training as needed. Provide process support to Downstream Processing (e.g., capture, intermediate...SuggéréTemps pleinRecrutement immédiat
- Senior SAP Basis Engineer (Remote) We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting... ...Support backup, recovery, and disaster recovery processes across SAP landscapes Collaborate with development, functional...SuggéréRemote job
- ...ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability. The PAM Engineer will act as a technical authority, owning PAM architecture, policies, onboarding standards, and operational governance. The role...Suggéré
- About the role We’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP...Suggéré
- ...Professional experience in pharmaceutical production as an operator/production technician etc Safety-conscious work Knowledge of process engineering Fluent English German knowledge an advantage What you will do: Work in various production functions while following...Suggéré
- ...You’ll be the proud owner of the Quality Management System, ensuring it’s not just a collection of binders, but a living, breathing engine of excellence. System Ownership: Take the wheel on Deviations, Change Control, Document Management, and Training. Risk...Suggéré
- ...Effectiveness Checks, as solutions to correct deviations and prevent future recurrence. Ensure cGMP compliance through the investigation process, and to drive their quality records to completion and timely closure. Support the business through ongoing change and process...Suggéré
- ...Contract type: Full-time Language: German (mandatory); English a strong plus The role Join a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ...SuggéréTemps plein
- ...this is your opportunity to grow in a dynamic GMP environment. As a Filling Operator you are a crucial pillar in our production process. Your area of responsibility includes: Operating our highly automated modern filling plant for liquid pharmaceuticals monitor the...SuggéréTemps pleinTravail postéQuart du jour
- ...Prepare manage and track CAPA plans including coordination with internal stakeholders and customers Own and manage core quality processes including Audit and Inspection Management Deviations CAPAs Change Control Document Management and Training Lead and support...SuggéréTemps plein
- ...practices during critical manufacturing steps (e.g. line clearance material dispensing equipment setup). Witness and verify critical process steps in-process controls (IPCs) and reconciliations. 2. Line Clearance and Batch Execution Monitoring Perform and document...SuggéréTemps pleinRecrutement immédiat
- ...seasoned quality leader who can not only manage complex quality processes but also drive cultural transformation build high-performing... ...apply sound risk management principles to QA decision-making and process optimization. Your profile We are looking for someone with...Temps plein
- ...is your opportunity to grow in a dynamic GMP environment. As a Compounding Operator you are a crucial pillar in our production process. Your area of responsibility includes: Control and execution of the manufacturing of product solutions on a pilot scale the core...Temps pleinTravail posté
- ...libraries according to current Good Manufacturing Practices (GMP) including supporting the investigation of new defects. Contribute to process improvements including the critical task of improving and reviewing batch records. Learn how to effectively perform risk...Temps pleinRecrutement immédiat